Relevant bibliographies by topics / Age-associated syndromes

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Age-associated syndromes'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Age-associated syndromes"

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Maetzler, Walter, Michael Drey, and Andreas H. Jacobs. "Sarkopenie und Frailty in der Neurologie. [Sarcopenia and frailty in neurology; Article in German]." Nervenarzt 86, no. 4 (2015): 420–30. https://doi.org/10.1007/s00115-014-4181-9.

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Sarcopenia and frailty are common geriatric syndromes and are associated with adverse health outcome and impaired health-related quality of life. Co-occurrences of these two syndromes with age-related neurological diseases are potentially high but not well investigated. Moreover, it is not well understood how these syndromes interact with neurological diseases, such as Parkinson's disease, Alzheimer's disease and stroke. This article introduces the currently most accepted concepts of sarcopenia and frailty, discusses the potential relevance of the syndromes for geriatric patients and p
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Watanabe, Takafumi, Shu Soeda, Yuta Endo, et al. "Rare Hereditary Gynecological Cancer Syndromes." International Journal of Molecular Sciences 23, no. 3 (2022): 1563. http://dx.doi.org/10.3390/ijms23031563.

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Hereditary cancer syndromes, which are characterized by onset at an early age and an increased risk of developing certain tumors, are caused by germline pathogenic variants in tumor suppressor genes and are mostly inherited in an autosomal dominant manner. Therefore, hereditary cancer syndromes have been used as powerful models to identify and characterize susceptibility genes associated with cancer. Furthermore, clarification of the association between genotypes and phenotypes in one disease has provided insights into the etiology of other seemingly different diseases. Molecular genetic disco
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Zhmyleva, Polina V. "Episodic syndromes associated with migraine (clinical and epidemiological study in pediatric practice)." Tambov Medical Journal 6, no. 2 (2024): 47–76. http://dx.doi.org/10.20310/2782-5019-2024-6-2-47-76.

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Abstract. Episodic syndromes of childhood that may be associated with migraine is an understudied condition rarely diagnosed in pediatric practice. The features of course in children of different age groups are not well described. The research purpose is to analyze the prevalence and characteristics of the course of childhood equivalents of migraine in children of various age groups in pediatric practice. Materials and methods. The study included the 1st (main) group of 250 children (120 (48 %) girls and 130 (52 %) boys) aged from 5 to 18 years (mean age – 13 (2.9) years, median age – 13 (11‒1
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Tikhonovich, Yulia V., Oleg A. Malievsky, and Anatoly Tyul'pakov. "Description of the first genetically confirming case with Donahue’s syndrome in Russia." Problems of Endocrinology 62, no. 2 (2016): 42–45. http://dx.doi.org/10.14341/probl201662242-45.

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Syndrome Donahue (leprechaunism) is a rare form of neonatal diabetes mellitus associated with INSR gene mutations. There are three types of insulin resistance syndrome: Donohue syndrome, Rabson—Mendenhall syndrome and insulin resistance type A. These syndromes are distinguished from one another by severity of symptoms, age of onset and age of death. Donohue and Rabson—Mendenhall syndromes are associated with biallelic mutations in the α-subunit or/and β-subunit of INSR gene and are characterized by more severe phenotype and poor prognosis. Patients with Donohue syndrome usually die within the
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Bihunyak, T. V., Yu I. Bondarenko, O. O. Кulyanda, S. M. Charnosh, A. S. Sverstiuk, and K. O. Bihuniak. "CHROMOSOMAL DISEASES IN THE HUMAN PATHOLOGY." International Journal of Medicine and Medical Research 6, no. 1 (2020): 50–60. http://dx.doi.org/10.11603/ijmmr.2413-6077.2020.1.11501.

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Background. Chromosomal diseases are the cause of 45-50 % of multiple birth defects. Basic research on mutations is performed using genomic technologies to identify a correlation between genotype and phenotype in aneuploidies and to understand its pathogenesis.
 Objective. The aim of the research is to study the etiology, pathogenesis of symptoms and diagnostics for patients with Down, Klinefelter, Turner syndromes and double aneuploidies by 21 and sex chromosomes.
 Methods. A literature review by the keywords “Down syndrome”, “Klinefelter syndrome”, “Turner syndrome”, “double aneupl
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Reilly, Colin, Lelia Murtagh, and Joyce Senior. "Factors Associated with Age of Diagnosis in Four Neurogenetic Syndromes." Journal of Policy and Practice in Intellectual Disabilities 14, no. 3 (2017): 180–86. http://dx.doi.org/10.1111/jppi.12202.

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Kozlova, Valentina M., Ekaterina E. Zelenova, Timur T. Valiev, Vera V. Semenova, Tatiana N. Nasedkina, and Svetlana N. Mikhailova. "Hereditary syndromes in pediatric hematooncology." Pediatric pharmacology 20, no. 6 (2024): 557–73. http://dx.doi.org/10.15690/pf.v20i6.2665.

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Hematooncological diseases head the list in the structure of malignant neoplasms of childhood. Somatic mutations in tumor clone cells have been well studied, included in modern classifications, and are used to stratify patients into prognostic risk groups and select a therapy program. At the same time, more than 50 hereditary syndromes associated with the development of hemoblastoses have been described. Some of them (Down’s syndrome, Klinefelter’s syndrome, microdeletion syndromes et al.) are caused by chromosomal pathology, while others describe alterations of one or more genes with differen
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Ivanova, N. V., E. E. Zelenova, V. G. Polyakov, et al. "Familial DICER1 syndrome with thyroid pathology. A series of clinical cases." Russian Journal of Pediatric Hematology and Oncology 10, no. 4 (2024): 49–60. http://dx.doi.org/10.21682/2311-1267-2023-10-4-49-60.

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Thyroid diseases in childhood occupy the second place after obesity in the structure of the general pathology of the endocrine system, eating disorders and metabolic disorders in children in the Russian Federation. Thyroid cancer in children makes up from 1.5 to 3 % of all malignant tumors, and from 8 to 22 % of malignant solid tumors of the head and neck, and the younger the child’s age, the more aggressive the disease proceeds.Familial forms of thyroid diseases may be associated with geographical features (living in iodine-deficient regions), but may also be part of hereditary syndromes, suc
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Papadopoulou-Marketou, Nektaria, Marina Tsoli, Eleftherios Chatzellis, Krystallenia I. Alexandraki, and Gregory Kaltsas. "Hereditary Syndromes Associated with Pancreatic and Lung Neuroendocrine Tumors." Cancers 16, no. 11 (2024): 2075. http://dx.doi.org/10.3390/cancers16112075.

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Pancreatic neuroendocrine tumors (PanNETs) and lung NETs (LNETs) represent a rare but clinically significant subgroup of neoplasms. While the majority is sporadic, approximately 17% of PanNETs and a subset of LNETs develop in the context of monogenic familial tumor syndromes, especially multiple endocrine neoplasia type 1 (MEN1) syndrome. Other inherited syndromes associated with PanNETs include MEN4, von Hippel–Lindau (VHL) syndrome, neurofibromatosis type 1 (NF1), and tuberous sclerosis complex (TSC). These syndromes are highly penetrant and their clinical manifestations may vary even among
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Khan, Sonia, and Raidah Al Baradie. "Epileptic Encephalopathies: An Overview." Epilepsy Research and Treatment 2012 (November 20, 2012): 1–8. http://dx.doi.org/10.1155/2012/403592.

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Epileptic encephalopathies are an epileptic condition characterized by epileptiform abnormalities associated with progressive cerebral dysfunction. In the classification of the International League Against Epilepsy eight age-related epileptic encephalopathy syndromes are recognized. These syndromes include early myoclonic encephalopathy and Ohtahara syndrome in the neonatal period, West syndrome and Dravet syndrome in infancy, myoclonic status in nonprogressive encephalopathies, and Lennox-Gastaut syndrome, Landau-Kleffner syndrome, and epilepsy with continuous spike waves during slow wave sle
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Dissertations / Theses on the topic "Age-associated syndromes"

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Jones, Melanie. "Mechanisms Associated with Aging and Age-Related Disease in Drosophila." VCU Scholars Compass, 2010. http://scholarscompass.vcu.edu/etd/2110.

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Aging is an intrinsic process that is independent of obvious disease. In contrast to normal aging, age-related diseases are conditions that typically manifest at advanced ages, are associated with explicit pathology and cause disability and premature death. We used Drosophila as a model to investigate the molecular-genetic mechanisms associated with aging and age-related disease. Age-related locomotor impairment (ARLI) is a serious condition for the elderly and greatly impacts their quality of life. Toward identifying genes and mechanisms that influence ARLI, we performed a forward genetic
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Books on the topic "Age-associated syndromes"

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Staedtke, Verena, and Eric H. Kossoff. Epilepsy Syndromes in Childhood. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0074.

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Epilepsy syndromes of childhood are a heterogeneous group of disorders that occur at specific neurodevelopmental stages, with a variable prognosis ranging from benign to catastrophic. In clinical practice they are categorized based on seizure type, age of onset, clinical presentation, electroencephalographic (EEG) findings, as well as response to treatment. In addition, recent advancements in neuroimaging and genetic testing have become important diagnostic tools revealing underlying defects for some of these syndromes. This knowledge has consequences for clinical practice, as it opens new per
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Shaibani, Aziz. Pseudoneurologic Syndromes. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0022.

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The term functional has almost replaced psychogenic in the neuromuscular literature for two reasons. It implies a disturbance of function, not structural damage; therefore, it defies laboratory testing such as MRIS, electromyography (EMG), and nerve conduction study (NCS). It is convenient to draw a parallel to the patients between migraine and brain tumors, as both cause headache, but brain MRI is negative in the former without minimizing the suffering of the patient. It is a “software” and not a “hardware” problem. It avoids irritating the patient by misunderstanding the word psychogenic whi
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Moeller, Friederike, Ronit M. Pressler, and J. Helen Cross. Genetic generalized epilepsy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0027.

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This chapter provides an overview of generalized epilepsies (GGE), which comprises a group of epilepsy syndromes of presumed genetic origin. They are classified into several syndromes according to their age, depending on clinical manifestation and associated electroencephalogram (EEG) features. The chapter introduces the concept of GGE before addressing different GGE syndromes, describing their clinical presentation, EEG features, treatment, prognosis, and underlying genetics. The following GGE syndromes are discussed in order of their age of onset—myoclonic astatic epilepsy, childhood absence
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Nita, Dragos A., Miguel A. Cortez, Jose Luis Perez Velazquez, and O. Carter Snead. Biological Bases of Symptomatic Generalized Epilepsies in Children. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0040.

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Symptomatic generalized epilepsies represent a group of challenging epilepsy syndromes, most often seen in children, which share the hallmark of a triad encompassing multiple seizure types, electroencephalographical (EEG) evidence of diffuse brain involvement, and dysfunction in the intellectual domain (global developmental delay or mental retardation). SGEs include the early myoclonic encephalopathy, early infantile epileptic encephalopathy (Ohtahara syndrome), West syndrome, epilepsy with myoclonic-astatic seizures, epilepsy with myoclonic absence, Lennox-Gastaut syndrome, and the progressiv
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Neary, John, and Neil Turner. Nutcracker syndrome and phenomenon. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0048.

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Nutcracker syndrome describes symptomatology associated with obstruction to the left renal vein caused by pressure from the overlying superior mesenteric artery. Modern imaging methods show that some degree of left renal vein obstruction may be a common incidental finding in asymptomatic patients so it is better described as ‘nutcracker phenomenon’, NCP. The association of NCP with symptoms and signs is often speculative. NCP may be seen at any age but most patients with symptoms attributed to it are teenagers or young adults. The strongest evidence is for association with episodic macroscopic
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Terplan, Mishka. Pain and Addiction in Women (DRAFT). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190265366.003.0032.

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Women experience pain differently than men and suffer unique pain conditions. Pain syndromes frequently overlap in women and can be associated with co-occurring mental health disorders, addiction, and intimate partner violence as well as childhood sexual abuse. A discussion of extant concepts for understanding pain in women includes gender-role theory, exposure theory, and vulnerability theory. The chapter focuses predominantly on women of child-bearing age, and their unique risks and management requirements; consequently, contraceptive needs and fulfillment are reviewed for their place in the
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Howe, Peter. Craniosynostosis Repair. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0028.

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Craniosynostosis is a condition in which one or more of the fibrous sutures in an infant skull fuses prematurely. This may lead to restricted skull and brain growth and elevated intracranial pressure. Many children with craniosynostosis undergo corrective cranioplasty in infancy, an age when the skull is relatively large in proportion to the rest of the body. Depending on the operation, it is common for blood loss to be substantial and exceed the child's estimated blood volume (EBV). Managing this blood loss is challenging and requires careful planning for fluid and blood product administratio
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Piggott, Margaret Ann. Neurochemical pathology of dementia. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199644957.003.0007.

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This chapter considers the neurodegenerative disorders Alzheimer’s disease (AD), Lewy body dementias (dementia with Lewy bodies (DLB) and Parkinson’s disease dementia(PDD)), frontotemporal dementia (FTD); and also vascular dementia (VaD) which results from cerebrovascular disease. These different conditions, which give rise to dementia syndromes, each have distinct neurochemical pathologies, with important implications for treatment. As increased age is the common risk factor generally associated with dementing illnesses, neurochemical changes are set in the context of the changes which occur
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Keat, Andrew. Oligoarticular disease. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0008.

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Oligoarthritis is a pattern of arthritis which most commonly resolves into a member of the spondyloarthritis family or sarcoidosis. Uncommonly it progresses to forms of arthritis more commonly associated with polyarthritis or monoarthritis and rarely it is associated with malignant or paraneoplastic syndromes. Three key aspects of diagnosis are consideration of possible diagnoses in the patient's age and ethnic groups; careful consideration of the personal and family history; and a search for and correct identification of characteristic associated features. This frequently involves collaborati
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Krishnan, Vaishnav, Bernard S. Chang, and Donald L. Schomer. The Application of EEG to Epilepsy in Adults and the Elderly. Edited by Donald L. Schomer and Fernando H. Lopes da Silva. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228484.003.0019.

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Surface or scalp electroencephalography (EEG) has become an indispensable tool for the diagnosis, classification, and care of patients with epilepsy across the age spectrum. This chapter provides an overview of interictal and corresponding ictal scalp EEG patterns observed in adults with certain classical epilepsy syndromes. In patients with one or more new-onset seizures, the value of EEG testing begins with a close examination of the interictal record. The morphology, frequency, and topography of interictal epileptiform discharges (when present) are typically sufficient to broadly distinguis
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Book chapters on the topic "Age-associated syndromes"

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Fechtner, Lisa, and Thorsten Pfirrmann. "Ubiquitin Ligases Involved in Progeroid Syndromes and Age-Associated Pathologies." In Proteostasis and Proteolysis. CRC Press, 2021. http://dx.doi.org/10.1201/9781003048138-07.

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Pehlivanoglu, Suray, and Sebnem Pehlivanoglu. "Craniosynostosis: Clinical Characteristics, Molecular Mechanisms and Treatment." In Molecular Approaches in Medicine. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359524.6.

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Craniosynostosis is a congenital condition marked by the early fusion of one or more cranial sutures. Cranial sutures are fibrous tissues that connect the skull bones. They play a crucial role in ensuring bone formation at the edges of the calvarial bones, which move apart to facilitate the passage of the head through the birth canal and allow for future brain growth. The premature fusion limits skull growth perpendicular to the affected sutures, potentially resulting in abnormal head shapes, increased intracranial pressure, and developmental delays. The prevalence of craniosynostosis is about
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Vieregge, P., G. Ziemens, A. Piosinski, M. Freudenberg, and D. Kömpf. "Parkinsonian features in advanced Down’s syndrome." In Age-associated Neurological Diseases. Springer Vienna, 1991. http://dx.doi.org/10.1007/978-3-7091-9135-4_19.

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Ainsbury, Elizabeth A., Ana Margarida Abrantes, Sarah Baatout, et al. "Individual Radiation Sensitivity and Biomarkers: Molecular Radiation Biology." In Radiobiology Textbook. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-18810-7_7.

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AbstractIn recent years, scientific understanding of the changes radiation makes to the various tissues of the body has vastly increased. Identification of biological markers of radiation exposure and response has become a wide field with an increasing interest across the radiation research community. This chapter introduces the concepts of individual radiosensitivity, radiosusceptibility, and radiodegeneration, which are the key factors to classify radiation responses. Biomarkers are then introduced, and their key characteristics as well as classification are explained, with a particular focu
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Engel, Andrew G., Kinji Ohno, and Steven M. Sine. "Congenital myasthenic Syndromes." In Myasthenia gravis And myasthenic disorders. Oxford University PressNew York, NY, 1999. http://dx.doi.org/10.1093/oso/9780195129700.003.0011.

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Abstract Congenital myasthenic syndromes (CMS) are neither new nor uncommon disorders. In 1937, Rothbart described four brothers under the age of 2 years with a myasthenic disorder, and by 1972 Sarah Bundey was able to collect 97 familial cases of myasthenia with onset before the age of 2 years. After the discovery of the autoimmune origin of myasthenia gravis (MG) in the 1970s and of the Lambert-Eaton syndrome in the 1980s, it became apparent that myasthenic disorders occurring in a familial or congenital setting must have a different pathogenesis. In the 1970s and 1980s, ultrastructural, cyt
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Adesina, Ore-ofe O., Sudama Reddi, Deborah I. Friedman, and Kathleen Digre. "Headache associated with high cerebrospinal fluid pressure." In Oxford Textbook of Headache Syndromes, edited by Michel Ferrari, Joost Haan, Andrew Charles, David W. Dodick, Fumihiko Sakai, and Christopher Kennard. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198724322.003.0039.

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Idiopathic intracranial hypertension (IIH) is a disorder of raised intracranial pressure, almost always associated with papilloedema, in the absence of underlying central nervous system pathology. It is a rare disease, with an annual incidence of around 1/100,000 persons with an onset between 11 and 58 years. It is predominantly seen in obese women of childbearing age (incidence 10–20/100,000), but can affect any age, race, or sex. The two morbidities associated with IIH are vision loss and headache, with headache ultimately affecting over 90% of patients. The exact mechanisms underlying IIH r
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Baraitser, Michael. "Cerebellar ataxia." In The Genetics of Neurological Disorders. Oxford University PressNew York, NY, 1997. http://dx.doi.org/10.1093/oso/9780192628145.003.0018.

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Abstract Major inroads have now been made by molecular geneticists into the differentiation of the many syndromes of cerebellar ataxia. In general, it is still useful to use age of onset and associated features as a starting point. Congenital onset: cerebellar hypoplasia recessive; cerebellar hypoplasia dominant; cerebellar hypoplasia affecting the granular layer; carbohydrate-deficient glycoprotein syndrome; pontoneocerebellar hypoplasia; Congenital onset affecting especially the vermis: Joubert’s syndrome;
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Bogduk, Nikolai. "Cervicogenic headache." In Oxford Textbook of Headache Syndromes, edited by Michel Ferrari, Joost Haan, Andrew Charles, David W. Dodick, Fumihiko Sakai, and Christopher Kennard. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198724322.003.0036.

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Idiopathic intracranial hypertension (IIH) is a disorder of raised intracranial pressure, almost always associated with papilloedema, in the absence of underlying central nervous system pathology. It is a rare disease, with an annual incidence of around 1 in 100,000 persons, with an age of onset between 11 and 58 years. It is predominantly seen in obese women of childbearing age (incidence 10–20 per 100,000), but can affect any age, ethnicity, or sex. The two morbidities associated with IIH are vision loss and headache, with headache ultimately affecting > 90% of patients. The exact mechani
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Pelzer, Nadine, Tobias Freilinger, and Gisela M. Terwindt. "Hemiplegic migraine and other monogenic migraine subtypes and syndromes." In Oxford Textbook of Headache Syndromes, edited by Michel Ferrari, Joost Haan, Andrew Charles, David W. Dodick, Fumihiko Sakai, and Christopher Kennard. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198724322.003.0008.

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Hemiplegic migraine (HM) is a rare monogenic subtype of migraine with aura that includes reversible motor weakness and can be either familial or sporadic. Three genes have been associated with HM. Migraine can also be part of more elaborate monogenic syndromes. When the family history includes early-onset cerebrovascular diseases and dementia, the monogenic small-vessel diseases CADASIL, RVCL-S, and COL4A1-associated syndromes should be considered. The mitochondrial disease MELAS is also associated with migraine-like and stroke-like episodes, often with a progressive nature, hearing loss and s
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Greggi T., Lolli F., Maredi E., et al. "Surgical Treatment For Scoliosis Associated With Rare Disease." In Studies in Health Technology and Informatics. IOS Press, 2012. https://doi.org/10.3233/978-1-61499-067-3-326.

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This is a retrospective study of 11 patients, 7 females and 4 males, treated at Our Department for an early onset scoliosis (EOS) associated with rare syndromes with growing spinal implants (Growing Rod or VEPTR-like) from 2006 to 2011. Mean follow-up was 24 months (range, 12 to 36). The mean age at surgery was 7. Patients were affected by Escobar's syndrome (1), scoliosis associated to congenital heart disease (1), Arnold Chiari type 1 (1), syringomyelia (1), NF 1 (2), Prader-Willi syndrome (1), trisomy 8 (1), arthrogryposis (2) and spondylo-rib dysplasia (1). Each patient was studied from th
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Conference papers on the topic "Age-associated syndromes"

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Silva, Mayana Cerqueira Martins da, Alfredo Guerra Netto, Camila Cardoso Barbosa, et al. "Pickardt syndrome." In II SEVEN INTERNATIONAL MEDICAL AND NURSING CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/iicongressmedicalnursing-018.

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Introduction: The Pickardt-Fahlbusch syndrome, very rare, is found in the group of endocrine syndromes of interruption of the pituitary nail, resulting in tertiary hypothyroidism. The pathophysiology is not fully elucidated, suggesting alterations of chromosomal orders. Case presentation: A 13-year-old female patient, born in Gama - DF, was admitted to the emergency room of the Santa Maria Regional Hospital (HRSM) with decreased level of consciousness associated with severe hypoglycemia, showing improvement after reversal of hypoglycemia. Discussion: There is a higher prevalence of Pickardt-Fa
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Baybuz, L. A., N. G. Perevalova, and V. Y. Makarov. "THE EFFECTIVENESS OF OZONE THERAPY IN THE REHABILITATION OF PATIENTS WITH DISORDERS OF THE CENTRAL NERVOUS SYSTEM AFTER SUFFERING COVID-ASSOCIATED PNEUMONIA." In The 16th «OCCUPATION and HEALTH» Russian National Congress with International Participation (OHRNC-2021). FSBSI “IRIOH”, 2021. http://dx.doi.org/10.31089/978-5-6042929-2-1-2021-1-54-58.

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Abstract: The consequences of the transferred new coronavirus infection are currently not well understood, but the neurotropicity of SARS-CoV-2 is beyond doubt. In the manifestations of postcoid syndrome, damage to the central nervous system is dominant and requires timely diagnosis and correction, incl. at the rehabilitation stage of medical care. The introduction of highly effective non-drug methods of treatment with a small number of side effects is an urgent task of modern medicine. Such methods of treatment can include ozone therapy - the use of an ozone-oxygen mixture (ACS) for therapeut
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Souza, Silas Paulo Lima de, Antonio Carlos Dias Andrade, Vinicius Leal Borges da Cruz, et al. "Relationship between stroke etiologies and clinical manifestations/Oxfordshire." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.634.

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Introduction: The classification of strokes subtypes is important, since they have different management and prognoses. This study aims to verify associations between the etiologies of the stroke according to the TOAST classification and the clinical presentation by the subtypes of the Oxfordshire scale. Methods: A descriptive cross-sectional study, with patients admitted to a stroke unit of a reference hospital in Salvador-BA between 11/2017 and 03/2020. We included patients over 18 years of age and didn’t include patients with inaccuracies in the filling of medical records or who didn’t meet
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Muniz, Camila Osterne, Bruna Araújo Fernandes, Beatriz Murta Melo Oliveira, et al. "Rates of hospitalizations for migraines and other cephalic algias syndromes is children between 2014 and 2020." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.700.

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Introduction: Migraine is the most common chronic headache in childhood, however, it is still little diagnosed in the pediatric group. Early crises can be very early, at 6 months of age. It may present in different ways according to the age group of the child and may or may not resemble the clinical picture of the associated manifestations that may aid in diagnosis. Methods and Objectives: The study used data available on the DataSus, in the category of hospitalization by the CID-10, in the group of less than 1 year, between 1 and 4 years, 5 and 9 years and 10 and 14 years, in the period from
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Lee, Annelise Akemi Higa, Felipe Teijeiro Cabral, Francisco Tomaz Meneses de Oliveira, and Rubens José Gagliardi. "Guillain Barré syndrome in late lupus: case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.557.

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Context: In the literature, there are few cases of Guillain Barré syndrome (GBS) in association with systemic lupus erythematosus (SLE). There is description of 19 neuropsychiatric syndromes associated with SLE, 12 of the central nervous system (CNS) and 7 of the peripheral nervous system (PNS). 10% of the patients with SLE and neurological manifestations have PNS complications. SLE is considered to have a late onset when it starts above 50 years of age and it consists in, on average, 26% of the total of individuals with SLE, however, in contrast to juvenile lupus, the number of studies is sca
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Meale, Emily, and Alexandra Fontaine. "A Systematic Review on Belimumab’s Effectiveness, Improved Health Outcomes and Quality of Life in Patients with Lupus Syndromes." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. http://dx.doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.93_2024.

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Autoimmune diseases are prevalent disorders that many individuals within the United States suffer from. Systemic lupus erythematosus (SLE) is a common autoimmune disease that has a high incidence in women of child-bearing age. Management for lupus depends on the anatomical location SLE manifests, the severity of disease, and the tolerance that one has for certain adverse effects. Glucocorticoids are commonly used to manage lupus. Currently, long term glucocorticoid usage is associated with devastating adverse effects, so current treatment options aim to mitigate corticosteroids use to improve
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Laden Hammoud, Shema El, Gabrielle Gruppelli Good, André Luiz Cristani Bizetto, and Anderson Matsubara. "Dissecção espontânea da artéria carótida em jovem: Um artigo de revisão." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.211.

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Background: Spontaneous dissection of the carotid artery is a significant cause of stroke in young people, and may be the etiology of up to 25% of ischemic strokes in this age group. Understanding the causes and clinical parameters about the disease is essential, since the perception of signs and symptoms that anticipate a cerebrovascular accident is an important prognostic factor. Objectives: Expand knowledge about the clinical and etiological mechanisms of spontaneous carotid dissection, in addition to the possibilities of diagnostic tools, providing an early approach to the disease. Methods
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Rocha, Ariane Silva da, Gisele Aparecida Fernandes, Cynthia Aparecida Bueno de Toledo Osório, Ruffo de Freitas-Júnior, and Maria Paula Curado. "Overall survival in patients with second primary breast cancer." In Brazilian Breast Cancer Symposium 2023. Mastology, 2023. http://dx.doi.org/10.29289/259453942023v33s1061.

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Objective: The objective of this study was to analyze the overall survival of patients with second primary synchronous and metachronous breast cancer. Methodology: A retrospective cohort study on women with second primary breast cancer, diagnosed between 2000 and 2015, was conducted. The cases were drawn from the Cancer Hospital registry and classified according to the hospital registry rules for second primary cancers. The second primary breast tumor was defined as synchronous or metachronous according to the diagnosis of the second cancer: ≤6 months of the first tumor and >6 months after
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Ramos, Júlia Xavier, Bruno Zacarias, Breno Barbosa, and Simone Brandão. "18-FDG PET ANALYSYS FOR DEMENTIA DIAGNOSIS- BASELINE RESULTS FROM A REFERENCE CENTER IN RECIFE, BRAZIL." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda061.

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Background: Positrons emission tomography associated with computed tomography- PET/CT using the 18 F-fluorodeoxyglucose is a well-established exam for the medical evaluation of dementia, mainly helping in differential diagnosis to determine the specific type of dementia. Objectives: To describe the role of the PET/CT in the differential diagnosis of dementia in patients. Methods: a single-center, descriptive and records-based analysis of patients with Dementia evaluated in a clinic of Neurology at Recife and referred to PET/ CT due to diagnosis uncertainty, between 2020-2021. Results: 29 patie
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Levine, P. H. "ACQUIRED IMMUNODEFICIENCY SYNDROME, HUMAN IMMUNODEFICIENCY VIRUS AND HEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644752.

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Less than 15 years ago the National Heart, Lung and Blood Institute surveyed physicians in the United States in order to characterize the demographics of hemophilia. The average age of persons with hemophilia in the United States was found to be 11.5 years old. By 10 years later, the life expectancy was predicted to be normal, and indeed the average age of persons with hemophilia in the U.S. is now in the early twenties. Early, intensive and predictably efficacious control of hemorrhage has made this result possible, and the therapeutic product which has allowed such control is commercial clot
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Reports on the topic "Age-associated syndromes"

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Brown, Antoinette Y. Improving delirium management in hospitalized elderly patients. University of Missouri - Columbia, 2024. https://doi.org/10.32469/10355/106341.

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Delirium is the leading complication in hospitalized older adults associated with increased mortality, adverse inpatient outcomes, and decreased functionality (McCusker et al., 2003). Delirium is a syndrome with various presentations, it can occur over a brief period, and patients may exhibit hallucinations or violence unpredictably (Tomlinson et al., 2017). Prevalence of delirium varies greatly secondary to patient demographics and comorbidities; the elderly and individuals with multiple chronic disease processes have an increased risk for inpatient delirium (Fuchs et al., 2020). Prevalence r
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Cao, Xianling, Xuanyou Zhou, Naixin Xu, Songchang Chang, and Chenming Xu. Association of IL-4 and IL-10 Polymorphisms with Preterm Birth Susceptibility: A Systematic Review and Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.4.0044.

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Review question / Objective: The aim of our systematic review and meta-analysis was to summarize the effects of IL-4 and IL-10 gene polymorphism and clarify their possible association with PTB. Condition being studied: World Health Organization (WHO) defines preterm birth (PTB) as babies born alive before 37 weeks of pregnancy are completed. The new estimates show that the prevalence of PTB during 2014 ranged from 8.7% to13.4% of all live births, about 15 million preterm babies born each year. Besides, PTB is the leading cause of death worldwide for children below 5 years of age. Babies born p
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Chou, Roger, Rongwei Fu, Tracy Dana, Miranda Pappas, Erica Hart, and Kimberly M. Mauer. Interventional Treatments for Acute and Chronic Pain: Systematic Review. Agency for Healthcare Research and Quality (AHRQ), 2021. http://dx.doi.org/10.23970/ahrqepccer247.

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Objective. To evaluate the benefits and harms of selected interventional procedures for acute and chronic pain that are not currently covered by the Centers for Medicare & Medicaid Services (CMS) but are relevant for and have potential utility for use in the Medicare population, or that are covered by CMS but for which there is important uncertainty or controversy regarding use. Data sources. Electronic databases (Ovid® MEDLINE®, PsycINFO®, the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews) to April 12, 2021, reference lists, and submission
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